Team:Paris/Notebook/Protocols

Extraction

• For each new extraction it's important to have a new bath of ETB
• Use a new blade for each extraction
• The band weight must be less than 200 mg

Amplification of promoters

=>To amplify the sequence in order to have enough amount of DNA to carry out the following of our experiments.

• Preparation of the templates : Resuspend of 1 colony in 100µl of water.
• Preparation of PCR mix :

For each samples, 1 µl dNTP
10 µl Buffer Phusion 5x
2,5 µl Oligo_F
2,5 µl Oligo_R
1µl template
1 µl Phusion
50 µl qsp H2O (33µl)

• make a mix with buffer, oligos and water for n+1 samples
• negative control : without template
• positive control : known template

• Program PCR : PROMOTEU

LID : 105°C
1. 98°C 30 sec initial denaturation
2. 98°C 10 sec denaturation
3. 60°C (depending of the size of oligos) 30 sec annealing
4. 72°C (1 min for 1 kb)
5. go to : 2 rep : 24-29
6. 72°C 5 min
7. sound : 1
8. hold : 10°C

Purification (Kit Promega)

Gel Slice and PCR Product Preparation

Dissolving the Gel Slice

• Following electrophoresis, excise DNA band from gel slice in a pre-weighed 1.5 mL microcentrifuge tube.
• Add 10µL membrane Binding Solution per 10 mg of gel slice. We prefer not to vortex and we incubate at 50-65°C until gel slice is completely dissolved (∼10 min). Quick centrifuge.

Processing PCR reactions

For products above 40 pb

• Add an equal volume of Membrane Binding Solution to the PCR reaction.

Binding of DNA

• Insert the SV Minicolumn into Collection Tube.
• Transfer dissolved gel mixture or prepared PCR product to the Minicolumn assembly. Incubate at room temperature for 1 minute.
• Centrifuge at 16,000 x g for 1 minute. Discard the flowthrough and reinsert Minicolumn into Collection Tube.

Washing

• Add 700 µL Membrane Wash Solution (ethanol added). Centrifuge at 16,000 x g for 1 minute. Discard flowthrough and reinsert the Minicolumn into Collection Tube.
• Repeat Step 4 with 500 µL Membrane Wash Solution. Centrifuge at 16,000 x g for 5 minutes.
• Empty the Collection Tube and recentrifuge the column assembly for 1 min with the microcentrifuge lid open (or off) to allow evaporation of any residual ethanol.

Elution

• Carefully transfer Minicolumn to a clean 1.5 mL microcentrifuge tube.
• Add 30 µL Buffer EB (Qiagen). Incubate at room temparature for 1 minute. Centifuge at 16,000 x g for 1 minute.
• Discard Minicolumn and store at 4 or -20°C.

Quantification by electrophoresis

• Gel : 1.5-2% agarose with BET added (5 µL BET for 100 mL TBE)
• 10 µL Quick-Load 1 kb DNA Ladder
• 2 µL LB + 3 µL DNA

Ligation

• 2 µL Ligase Buffer 10X
• X µg/µL vector
• 3 or 4 x X µg/µL insert
• Pure water qsp 20 µL
• 1 µL T4 ligase
• O/N at 16°C

Transformation

Use of TOP10 chemically competent cells

• Defroze competent cells on ice during 5'
• Add 5µl of DNA Ligation in 50µL of competent bacterias (or 1µL for the positive control puc19)
• Incubate 30' on ice
• Heat-shock the cells during 30" at 42°C without shaking
• Put 2' on ice
• Add 250µL of pre-warmed SOC medium (42°C)
• Incubate 1h at 37°C under shaking (225rpm)
• Spin at 5.000rpm during 30"
• Remove 150µL of supernatant
• Resuspend the pellet in the 150µL left
• Spread on adequated plates
• Incubate O/N at 37°C

PCR Screening

Use of 8 clones of Ligation transformants for screening PCR

• One toothpick of each clone's colony per PCR tube
• Use toothpick to start 7.5mL O/N culture

After, add

• 25µL Mix
• 1µL Oligo F (10µM)
• 1µL Oligo R (10µM)
• 23µL pure water
• negative control : without clone's colony
• positive control

• Program : SCREENIN

LID 105°C
1. 95°C 5min
2. 95°C 30 sec
3. 55°C 30 sec
4. 72°C (1 min for 1kb)
5. go to : 2 rep : 29
6. sound : 1
7. hold : 4°C

Electrophoresis Purification of PCR

• 10µl of ladder 100 pb or 1 kb
• 4 µl of screening PCR
• Migration at 100V on 1,5% gel until 3/4 way

Sequencing

voir ici -> [http://institut.cochin.inserm.fr/rubric_recherche/Plates-Formes/sequencage_genomique/I18NFolder.2005-02-10.4781618697/page2/fr Sequencing COCHIN]

Promoter Characterization Plan

For theoretical consideration, see estimation of parameters

Standart construct

        Tested promoter - B0032 - E0040 - B0010 - B0012

attention le tableau ne correspond pas au titre, j'y travaille... Ana :-)

• Summary table

This table contains the promoters we need to characterize, the transcription factors whose effect on the promoter we want to test, and the plasmid we want to obtain in order to carry out each characterization